Canonical Allele Identifier: CA1931452347

Gene: COX15 CUTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713755_99713756delinsAG , CM000672.2:g.99713755_99713756delinsAG	GRCh38
NC_000010.10:g.101473512_101473513delinsAG , CM000672.1:g.101473512_101473513delinsAG	GRCh37
NC_000010.9:g.101463502_101463503delinsAG	NCBI36
NG_008986.1:g.23911_23912delinsCT , LRG_406:g.23911_23912delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*831_*832delinsCT (COX15) MANE Select	ENSP00000016171.6:n.*831_*832delinsCT
ENST00000649102.1:c.*460+2592_*460+2593delinsCT	ENSP00000497114.1:n.*460+2592_*460+2593delinsCT
ENST00000016171.5:c.*831_*832delinsCT (COX15)	ENSP00000016171.5:n.*831_*832delinsCT
ENST00000370483.9:c.1102-277_1102-276delinsCT (COX15)	ENSP00000359514.5:n.1102-277_1102-276delinsCT
ENST00000493385.5:n.117-9163_117-9162delinsAG (CUTC)
NM_004376.5:c.1102-277_1102-276delinsCT , LRG_406t2:c.1102-277_1102-276delinsCT (COX15)	NP_004367.2:n.1102-277_1102-276delinsCT
NM_078470.4:c.*831_*832delinsCT , LRG_406t1:c.*831_*832delinsCT (COX15)	NP_510870.1:n.*831_*832delinsCT
XM_005269539.3:c.1101+2592_1101+2593delinsCT (COX15)	XP_005269596.1:n.1101+2592_1101+2593delinsCT
XM_006717633.2:c.*1012_*1013delinsCT (COX15)	XP_006717696.1:n.*1012_*1013delinsCT
XM_006717634.2:c.*49+2592_*49+2593delinsCT (COX15)	XP_006717697.1:n.*49+2592_*49+2593delinsCT
XM_011539298.1:c.*50-277_*50-276delinsCT (COX15)	XP_011537600.1:n.*50-277_*50-276delinsCT
NM_001320974.1:c.1101+2592_1101+2593delinsCT (COX15)	NP_001307903.1:n.1101+2592_1101+2593delinsCT
NM_001320975.1:c.*1012_*1013delinsCT (COX15)	NP_001307904.1:n.*1012_*1013delinsCT
NM_001320976.1:c.*831_*832delinsCT (COX15)	NP_001307905.1:n.*831_*832delinsCT
NM_004376.6:c.1102-277_1102-276delinsCT (COX15)	NP_004367.2:n.1102-277_1102-276delinsCT
NM_078470.5:c.*831_*832delinsCT (COX15)	NP_510870.1:n.*831_*832delinsCT
XM_006717634.3:c.*49+2592_*49+2593delinsCT (COX15)	XP_006717697.1:n.*49+2592_*49+2593delinsCT
XM_011539298.2:c.*50-277_*50-276delinsCT (COX15)	XP_011537600.1:n.*50-277_*50-276delinsCT
NM_001320974.2:c.1101+2592_1101+2593delinsCT (COX15)	NP_001307903.1:n.1101+2592_1101+2593delinsCT
NM_001320975.2:c.*1012_*1013delinsCT (COX15)	NP_001307904.1:n.*1012_*1013delinsCT
NM_001320976.2:c.*831_*832delinsCT (COX15)	NP_001307905.1:n.*831_*832delinsCT
NM_001372024.1:c.*50_*51delinsCT (COX15)	NP_001358953.1:n.*50_*51delinsCT
NM_001372025.1:c.*831_*832delinsCT (COX15)	NP_001358954.1:n.*831_*832delinsCT
NM_001372026.1:c.*831_*832delinsCT (COX15)	NP_001358955.1:n.*831_*832delinsCT
NM_001372027.1:c.*935_*936delinsCT (COX15)	NP_001358956.1:n.*935_*936delinsCT
NM_001372028.1:c.*258_*259delinsCT (COX15)	NP_001358957.1:n.*258_*259delinsCT
NM_004376.7:c.1102-277_1102-276delinsCT (COX15)	NP_004367.2:n.1102-277_1102-276delinsCT
NM_078470.6:c.*831_*832delinsCT (COX15) MANE Select	NP_510870.1:n.*831_*832delinsCT
NR_164009.1:n.1904_1905delinsCT (COX15)